# Medi-Dyne, Inc.

- Location (FDA's records): Glens Falls, NY
- FDA decisions: 4 (1993–2000): 4 510(k) clearances
- Product codes: DQO (3), DQY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Curative Medical Technology, Inc.: 1 (https://510kreport.com/company/curative-medical-technology)

## Its most-cited devices
- K000825: 4F-7F Medi-Dyne Torq Flow XLB Angiographic Catheter (2000), cited by 1

## Recent decisions
- K000825: 4F-7F Medi-Dyne Torq Flow XLB Angiographic Catheter (Sep 21, 2000)
- K970401: Medi-Dyne Guiding Catheter (Aug 1, 1997)
- K931833: Modified Luer (Sep 28, 1993)
- K930694: Medi-Dyne Angiographic Catheter (Aug 2, 1993)

Source page: https://510kreport.com/company/medi-dyne